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Diseases
Genes (1032)
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TBX5
Holt–oram Syndrome
IFIH1
Singleton Merten Syndrome
SLC20A2
Primary Familial Brain Calcification
PDGFRB
Primary Familial Brain Calcification
AGGF1
Klippel-Trenaunay-Weber Syndrome
PDGFB
Primary Familial Brain Calcification
SMOC1
Klippel-Trenaunay-Weber Syndrome
Oral Allergy Syndrome
Holt–oram Syndrome
KLK3
Benign Prostatic Hyperplasia (Bph)
SRD5A2
Benign Prostatic Hyperplasia (Bph)
ITGB3
Coronary Thrombosis
CNNM2
Tetany
DDX58
Singleton Merten Syndrome
SALL4
Holt–oram Syndrome
PLAT
Coronary Thrombosis
CST1
Hay Fever
FGF7
Benign Prostatic Hyperplasia (Bph)
PRL
Benign Prostatic Hyperplasia (Bph)
NPY
Nasal Congestion
RSPH4A
Nasal Congestion
XPR1
Primary Familial Brain Calcification